Key result
In seemingly healthy 71-year-old men, elevated cardiac troponin I concentrations were independently associated with higher levels of NT-proBNP (p<0.001).
Why the study?
Do minor elevations of hypersensitive cardiac troponin I correlate with elevated NT-proBNP and other biomarkers of target organ damage in seemingly healthy elderly men?
Observational (n=1,205)
Do minor elevations of hypersensitive cardiac troponin I correlate with elevated NT-proBNP and other biomarkers of target organ damage in seemingly healthy elderly men?
Minor elevations in hypersensitive cardiac troponin I in seemingly healthy elderly men are independently associated with elevated NT-proBNP, suggesting unrecognized subclinical myocardial pathology.
Minor troponin elevations may reflect subclinical cardiac injury; leaves open prognostic value and need for prospective trials.
BACKGROUND: Hypersensitive cardiac troponin I (cTnI) assays detect even minor elevations of cTnI. Previous findings identifying a group of seemingly healthy elderly men with very minor elevations of cTnI have shown that these men were at risk of premature cardiovascular death. OBJECTIVES: To study the association between cTnI concentrations and cardiovascular risk factors and subclinical cardiac and renal target organ damage in a community-based sample of elderly men. METHODS: Biomarkers reflecting glucose and lipid metabolism, renal function, cardiac function and inflammation were measured in the ULSAM study (n = 1205, mean age 71 years). The participants were placed in three subgroups based on the cTnI concentrations: a low group with cTnI <0.02 microg/L, an intermediate group with cTnI between 0.02 and 0.039 microg/L and a high group with cTnI >0.039 microg/L. RESULTS: In the entire cohort of 71-year-old men, most markers of glucose and lipid metabolism, renal function, inflammation and NT-proBNP were significantly related to the concentrations of cTnI, and most obviously in the high-cTnI group. In subjects with no signs of CVD (cardiovascular disease), only levels of NT-proBNP related to cTnI, and with the highest NT-proBNP levels in the high-cTnI group (p<0.01). A multiple regression analysis showed that NT-proBNP was independently related to cTnI (p<0.001). CONCLUSIONS: Measurement of cardiac troponins with highly sensitive assays identifies those at risk of premature CVD death who have hitherto remained unrecognized. The associated elevations of NT-proBNP in these participants support the fact that these elevations reflect ongoing pathological processes in the myocardium.
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Venge et al. (2009) conducted an observational in Seemingly healthy elderly men (n=1,205). Elevated cardiac troponin I (cTnI) vs. Low cTnI (<0.02 microg/L) was evaluated on Association between cTnI concentrations and NT-proBNP levels (p=<0.001). In seemingly healthy 71-year-old men, elevated cardiac troponin I concentrations were independently associated with higher levels of NT-proBNP (p<0.001).
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